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Kasabach-Merritt syndrome

Kasabach-Merritt syndrome
Classification & external resources
ICD-9 287.39
OMIM 141000
DiseasesDB 30701
eMedicine med/1221  ped/1234

Kasabach-Merritt Syndrome (KMS) is a rare disease, usually of infants, in which a vascular tumor leads to decreased platelet counts and sometimes other bleeding problems,[1] which can be life-threatening.[2] It is also known as hemangioma thrombocytopenia syndrome.



KMS is usually caused by a hemangioendothelioma or other vascular tumor, often present at birth.[3][4] Although these tumors are relatively common, it is rare for them to cause KMS.

When these tumors are large or are growing rapidly, sometimes they can trap platelets, causing severe thrombocytopenia. The combination of vascular tumor and consumptive thrombocytopenia defines KMS. Tumors can be found in the trunk, upper and lower extremities, retroperioneum, and in the cervical and facial areas.[1]

This consumptive coagulopathy also uses up clotting factors, such as fibrinogen which may worsen bleeding. The coagulopathy can progress to disseminated intravascular coagulation and even death.[1]

Diagnostic workup

The diagnostic workup[5] is directed by the presenting signs and symptoms, and can involve:

  • blood counts, clotting studies, and other laboratory testing
  • imaging tests (ultrasound, CT scan, MRI, sometimes angiography, and rarely nuclear medicine scans)
  • biopsy of the tumor.

Patients uniformly show severe thrombocytopenia, low fibrinogen levels, high fibrin degradation products (due to fibrinolysis), and microangiopathic hemolysis.[1]


Management of KMS, particularly in severe cases, can be complex and require the joint effort of multiple subspecialists. This is a rare disease with no consensus treatment guidelines or large randomized controlled trials to guide therapy.

Supportive care

Patients with KMS can be extremely ill and may need intensive care. They are at risk of bleeding complications including intracranial hemorrhage. The thrombocytopenia and coagulopathy are managed with platelet transfusions and fresh frozen plasma, although caution is needed due to the risk of fluid overload and heart failure from multiple transfusions. The possibility of disseminated intravascular coagulation, a dangerous and difficult-to-manage condition, is concerning. Anticoagulant and antiplatelet medications can be used after careful assessment of the risks and benefits.[5]

Definitive treatment

Generally, treatment of the underlying vascular tumor results in resolution of KMS. If complete surgical resection is feasible, it provides a good opportunity for cure (although it can be dangerous to operate on a vascular tumor in a patient prone to bleeding, even with appropriate surgical subspecialists involved).[5]

If surgery is not possible, various other techniques [1] can be used to control the tumor:


KMS has a mortality rate of about 30%. For patients that survive the acute disease, supportive care may be required through a gradual recovery.

Furthermore, patients may need care from a dermatologist or plastic surgeon for residual cosmetic lesions. On long-term followup, most patients have skin discoloration and/or mild disfiguration from the dormant tumor.[6]


  1. ^ a b c d e Hall G (2001). "Kasabach-Merritt syndrome: pathogenesis and management.". Br J Haematol 112 (4): 851-62. PMID 11298580.
  2. ^ Shim W (1968). "Hemangiomas of infancy complicated by thrombocytopenia.". Am J Surg 116 (6): 896-906. PMID 4881491.
  3. ^ Enjolras O, Wassef M, Mazoyer E, Frieden I, Rieu P, Drouet L, Taïeb A, Stalder J, Escande J (1997). "Infants with Kasabach-Merritt syndrome do not have "true" hemangiomas.". J Pediatr 130 (4): 631-40. PMID 9108863.
  4. ^ el-Dessouky M, Azmy A, Raine P, Young D (1988). "Kasabach-Merritt syndrome.". J Pediatr Surg 23 (2): 109-11. PMID 3278084.
  5. ^ a b c Krafchik, Bernice R (2005-12-19). Kasabach-Merritt Syndrome. eMedicine - Hematology. WebMD. Retrieved on 2006-05-15.
  6. ^ Enjolras O, Mulliken J, Wassef M, Frieden I, Rieu P, Burrows P, Salhi A, Léauté-Labrèze C, Kozakewich H (2000). "Residual lesions after Kasabach-Merritt phenomenon in 41 patients.". J Am Acad Dermatol 42 (2 Pt 1): 225-35. PMID 10642677.
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Kasabach-Merritt_syndrome". A list of authors is available in Wikipedia.
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